Variant report

Variant	nsv602962
Chromosome Location	chr6:38907202-38940282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:38936310-38936447	K562	blood:	n/a	n/a
2	ATF1	chr6:38919623-38919663	K562	blood:	n/a	n/a
3	ATF1	chr6:38936497-38936730	K562	blood:	n/a	n/a
4	ATF1	chr6:38907941-38908103	K562	blood:	n/a	n/a
5	BACH1	chr6:38936526-38936631	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr6:38936672-38937015	Hela-S3	cervix:	n/a	chr6:38936813-38936824
7	CEBPB	chr6:38915477-38915639	K562	blood:	n/a	chr6:38915498-38915509
8	CEBPB	chr6:38936672-38936956	HepG2	liver:	n/a	chr6:38936813-38936824
9	CEBPB	chr6:38936660-38936909	K562	blood:	n/a	chr6:38936813-38936824
10	CEBPB	chr6:38936663-38936930	IMR90	lung:	n/a	chr6:38936813-38936824
11	CEBPB	chr6:38915434-38915634	H1-hESC	embryonic stem cell:	n/a	chr6:38915498-38915509
12	CEBPB	chr6:38936699-38936899	A549	lung:	n/a	chr6:38936813-38936824
13	CEBPB	chr6:38915428-38915641	HepG2	liver:	n/a	chr6:38915498-38915509
14	CTCF	chr6:38911860-38912010	GM12867	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
15	CTCF	chr6:38911880-38912030	HEK293	kidney:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
16	CTCF	chr6:38911900-38912050	HCT-116	colon:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
17	CTCF	chr6:38911872-38912018	GM19238	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
18	CTCF	chr6:38911880-38912030	GM12875	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
19	CTCF	chr6:38937640-38937790	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr6:38911840-38911990	AG09309	skin:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
21	CTCF	chr6:38911900-38912050	GM12864	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
22	CTCF	chr6:38937540-38937690	HEK293	kidney:	n/a	n/a
23	CTCF	chr6:38911840-38911990	HMEC	breast:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
24	CTCF	chr6:38911900-38912050	GM12865	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
25	CTCF	chr6:38911840-38911990	GM12868	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
26	CTCF	chr6:38916740-38916890	GM12867	blood:	n/a	n/a
27	CTCF	chr6:38911920-38912070	RPTEC	kidney:	n/a	chr6:38911927-38911945
28	CTCF	chr6:38911824-38911988	HepG2	liver:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
29	CTCF	chr6:38911836-38912043	MCF-7	breast:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
30	CTCF	chr6:38911879-38911925	GM13976	blood:	n/a	n/a
31	CTCF	chr6:38911760-38911910	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr6:38911817-38912064	MCF-7	breast:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
33	CTCF	chr6:38911910-38911966	GM13977	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
34	CTCF	chr6:38911860-38912010	GM06990	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
35	CTCF	chr6:38911880-38912030	SAEC	small airway:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
36	CTCF	chr6:38911860-38912010	HepG2	liver:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
37	CTCF	chr6:38911860-38912010	GM12878	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
38	CTCF	chr6:38911860-38912010	GM12869	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
39	CTCF	chr6:38911880-38912030	GM12864	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
40	CTCF	chr6:38911840-38911990	GM12878	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
41	CTCF	chr6:38911860-38912010	BE2_C	brain:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
42	CTCF	chr6:38911780-38911930	GM06990	blood:	n/a	chr6:38911919-38911927
43	CTCF	chr6:38911896-38912006	Fibrobl	skin:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
44	CTCF	chr6:38911864-38911998	HepG2	liver:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
45	CTCF	chr6:38911860-38912010	HRPEpiC	eye:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
46	CTCF	chr6:38911876-38912019	GM12892	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
47	CTCF	chr6:38911882-38911998	GM19239	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
48	CTCF	chr6:38911920-38912070	GM12866	blood:	n/a	chr6:38911927-38911945
49	CTCF	chr6:38911915-38911947	Medullo	brain:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934
50	CTCF	chr6:38911820-38911970	GM12866	blood:	n/a	chr6:38911919-38911927 chr6:38911919-38911932 chr6:38911927-38911945 chr6:38911916-38911934

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:38921683-38921733	SK-N-SH_RA	brain:	n/a
2	chr6:38921683-38921733	AG04450	lung:	fetal
3	chr6:38921683-38921733	HUVEC	blood vessel:	n/a
4	chr6:38921683-38921733	HCT-116	colon:	n/a
5	chr6:38921683-38921733	HIPEpiC	eye:	n/a
6	chr6:38921683-38921733	SK-N-SH	brain:	n/a
7	chr6:38921683-38921733	Hepatocyte	liver:	n/a
8	chr6:38921683-38921733	ProgFib	skin:	n/a
9	chr6:38921683-38921733	NB4	blood:	n/a
10	chr6:38921683-38921733	AG09319	gingival:	n/a
11	chr6:38921683-38921733	A549	lung:	n/a
12	chr6:38921683-38921733	NT2-D1	testis:	n/a
13	chr6:38921683-38921733	Hela-S3	cervix:	n/a
14	chr6:38921683-38921733	HCM	heart:	n/a
15	chr6:38921683-38921733	GM06990	blood:	n/a
16	chr6:38921683-38921733	AG09309	skin:	n/a
17	chr6:38921683-38921733	GM19239	blood:	n/a
18	chr6:38921683-38921733	PANC-1	pancreas:	n/a
19	chr6:38921683-38921733	PrEC	prostate:	n/a
20	chr6:38921683-38921733	HNPCEpiC	eye:	n/a
21	chr6:38921683-38921733	CMK	blood:	n/a
22	chr6:38921683-38921733	HAEpiC	amniotic membrane:	n/a
23	chr6:38921683-38921733	BE2_C	brain:	n/a
24	chr6:38921683-38921733	HPAEpiC	pulmonary alveolar:	n/a
25	chr6:38921683-38921733	T-47D	breast:	n/a
26	chr6:38921683-38921733	H1-hESC	embryonic stem cell:	embryo
27	chr6:38921683-38921733	NHBE	bronchial:	n/a
28	chr6:38921683-38921733	AG10803	skin:	n/a
29	chr6:38921683-38921733	IMR90	lung:	fetal
30	chr6:38921683-38921733	AoSMC	blood vessel:	n/a
31	chr6:38921683-38921733	HepG2	liver:	n/a
32	chr6:38921683-38921733	U87	brain:	n/a
33	chr6:38921683-38921733	NHDF-neo	bronchial:	n/a
34	chr6:38921683-38921733	HRPEpiC	eye:	n/a
35	chr6:38921683-38921733	GM12891	blood:	n/a
36	chr6:38921683-38921733	Jurkat	blood:	n/a
37	chr6:38921683-38921733	HCPEpiC	choroid plexus:	n/a
38	chr6:38921683-38921733	LNCaP	prostate:	n/a
39	chr6:38921683-38921733	AG04449	skin:	fetal
40	chr6:38921683-38921733	PFSK-1	brain:	n/a
41	chr6:38921683-38921733	HL-60	blood:	n/a
42	chr6:38921683-38921733	ovcar-3	ovarian:	n/a
43	chr6:38921683-38921733	MCF-7	breast:	n/a
44	chr6:38921683-38921733	HCF	heart:	n/a
45	chr6:38921683-38921733	HMEC	breast:	n/a
46	chr6:38921683-38921733	SKMC	muscle:	n/a
47	chr6:38921683-38921733	SAEC	small airway:	n/a
48	chr6:38921683-38921733	HEK293	kidney:	embryo
49	chr6:38921683-38921733	ECC-1	luminal epithelium:	n/a
50	chr6:38921683-38921733	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:38902804..38905532-chr6:38908040..38910496,2	K562	blood:
2	chr6:38839762..38840315-chr6:38911448..38912424,2	MCF-7	breast:
3	chr6:38934741..38936465-chr6:38939691..38941854,2	K562	blood:
4	chr6:38939668..38941967-chr6:39077128..39080057,2	K562	blood:
5	chr6:38914946..38917394-chr6:38943758..38945918,2	MCF-7	breast:
6	chr6:38901008..38902530-chr6:38905671..38907488,2	K562	blood:
7	chr6:38934741..38936465-chr6:38939691..38941854,2	K562	blood:
8	chr6:38909328..38913522-chr6:38913862..38917283,4	K562	blood:
9	chr6:38939906..38942695-chr6:38942827..38945177,2	K562	blood:
10	chr6:38909328..38913522-chr6:38913862..38917283,4	K562	blood:
11	chr6:38911849..38912730-chr6:39126712..39127584,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAYSD1-1	chr6:38914899-38915050	NONHSAT112341

Variant related genes	Relation type
ENSG00000231150	TF binding region
ENSG00000231150	CpG island
ENSG00000217165	chromatin interactions
ENSG00000112167	chromatin interactions

Extended variants
information (count: 496 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12190140	chr6:38907202-38907203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377379654	chr6:38907220-38907221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs75391839	chr6:38907233-38907234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs16891295	chr6:38907291-38907292	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs188269884	chr6:38907370-38907371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140314443	chr6:38907437-38907438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559725321	chr6:38907456-38907457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145789043	chr6:38907465-38907466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547997908	chr6:38907495-38907496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548545800	chr6:38907496-38907497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138382769	chr6:38907500-38907501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149192566	chr6:38907518-38907519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143379313	chr6:38907519-38907520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12664669	chr6:38907529-38907530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538991741	chr6:38907567-38907568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148381082	chr6:38907625-38907626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs16891298	chr6:38907626-38907627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371067614	chr6:38907742-38907743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs55675276	chr6:38907753-38907754	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs112844203	chr6:38907766-38907767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559911032	chr6:38907797-38907798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573539391	chr6:38907894-38907895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78259068	chr6:38907906-38907907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376178534	chr6:38907914-38907915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150836809	chr6:38907920-38907921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563576097	chr6:38907933-38907934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531530371	chr6:38907946-38907947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138383632	chr6:38907999-38908000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192171770	chr6:38908039-38908040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs56247488	chr6:38908044-38908045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74968604	chr6:38908064-38908065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374114898	chr6:38908074-38908075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567851980	chr6:38908113-38908114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574119685	chr6:38908142-38908143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530268384	chr6:38908179-38908180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550126910	chr6:38908183-38908184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115523768	chr6:38908285-38908286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184012361	chr6:38908289-38908290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75272048	chr6:38908290-38908291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1332011	chr6:38908311-38908312	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs547652097	chr6:38908405-38908406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112992030	chr6:38908419-38908420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554603318	chr6:38908440-38908441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188842873	chr6:38908448-38908449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542385534	chr6:38908482-38908483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs579786	chr6:38908515-38908516	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs558817854	chr6:38908538-38908539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369266662	chr6:38908557-38908558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116196609	chr6:38908568-38908569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115253867	chr6:38908589-38908590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Glioblastoma multiforme	21510904	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38906800-38909800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr6:38909600-38909800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr6:38909800-38910000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
4	chr6:38910000-38910800	Enhancers	Liver	Liver
5	chr6:38910200-38910600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:38910200-38910800	Enhancers	Gastric	stomach
7	chr6:38910800-38911800	Weak transcription	Gastric	stomach
8	chr6:38911800-38912200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr6:38911800-38912200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:38912000-38912200	Enhancers	Gastric	stomach
11	chr6:38912200-38912600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:38912600-38913000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:38912600-38913000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
14	chr6:38923600-38924000	Bivalent Enhancer	Right Ventricle	heart
15	chr6:38923600-38924200	Bivalent Enhancer	Adipose Nuclei	Adipose
16	chr6:38923600-38924200	Bivalent Enhancer	Left Ventricle	heart
17	chr6:38923600-38924200	Enhancers	Pancreas	Pancrea
18	chr6:38923600-38924400	Enhancers	Liver	Liver
19	chr6:38923600-38925000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr6:38923800-38924400	Enhancers	Brain Anterior Caudate	brain
21	chr6:38924000-38924200	Bivalent Enhancer	Stomach Mucosa	stomach
22	chr6:38924000-38924400	ZNF genes & repeats	Fetal Intestine Small	intestine
23	chr6:38924200-38924400	Enhancers	Adipose Nuclei	Adipose
24	chr6:38925000-38925800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr6:38925400-38925800	Enhancers	NHEK	skin
26	chr6:38925800-38926000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr6:38925800-38926000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:38926000-38926800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr6:38926600-38926800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:38926800-38927000	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr6:38933000-38933600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:38933000-38933600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:38936400-38936800	Enhancers	K562	blood
34	chr6:38938200-38939200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:38938200-38942200	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr6:38938400-38938600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
37	chr6:38939000-38939200	Enhancers	Fetal Intestine Large	intestine
38	chr6:38939200-38941400	Weak transcription	Fetal Intestine Large	intestine
39	chr6:38939600-38939800	Enhancers	Fetal Intestine Small	intestine
40	chr6:38939800-38941400	Weak transcription	Fetal Intestine Small	intestine

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